• BMC anesthesiology · Mar 2023

    Randomized Controlled Trial

    95% effective volume of ropivacaine for ultrasound‑guided supra‑inguinal fascia iliaca compartment block.

    • Can Zhang, Wei Dai, and Kaihua He.
    • anesthesiology department, The First Affiliated Hospital of Chongqing Medical University, Chongqing, China.
    • BMC Anesthesiol. 2023 Mar 29; 23 (1): 9898.

    BackgroundHip arthroplasty is effective in treating hip diseases, such as osteoarthritis and hip fracture, but it often brings severe trauma and pain. In recent years, ultrasound-guided supra-inguinal fascia iliaca compartment block(S-FICB) has become a widely used nerve block method for analgesia in hip arthroplasty.MethodsFifty-three patients preparing for hip arthroplasty were prospectively enrolled. S-FICB was performed under ultrasound guidance, and inject 0.33% ropivacaine into the space. Using the biased-coin design (BCD) sequential allocation method. The initial volume of 0.33% ropivacaine was 30ml. In case of failure, the next patient received a higher volume (defined as the previous volume with an increment of 1.2 mL). If the previous patient had a successful block, the next patient was randomized to a lower volume (defined as the previous volume with a decrement of 1.2 mL), with a probability of b = 0.05, or the same volume, with a probability of 1 - b = 0.95. The study was stopped when 45 successful blocks were achieved.ResultsForty-five patients (84.9%) were blocked successfully. The 95% effective volume (EV95) was 34.06ml (95%CI 33.35 ~ 36.28ml). There were 31 patients with non-fracture in this study. The quadriceps muscle strength decreased in only two patients. Moreover, they both received 34.8ml of ropivacaine for S-FICB. Twenty-two patients had hip fractures. There were 3 patients (14%) with failed blocks and 19 patients (86%) with successful blocks. However, all fracture patients experienced less pain after S-FICB.ConclusionEV95 of 0.33% ropivacaine for ultrasound-guided S-FICB was 34.06ml.Trial RegistrationThe trial was registered at the Chinese Clinical Trial Registry (registration number: ChiCTR2100052214, registration date: 2021 October 22).© 2023. The Author(s).

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